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Benzenesulfonamide, N-[4-(phenylamino)phenyl]-, also known as N-(4-phenylaminophenyl)benzenesulfonamide, is an organic compound with the chemical formula C12H12N2O2S. It is a derivative of benzenesulfonamide, featuring a phenylamino group attached to the para position of the benzene ring. Benzenesulfonamide, N-[4-(phenylamino)phenyl]- is characterized by its white crystalline appearance and is soluble in organic solvents. It has potential applications in the synthesis of pharmaceuticals and dyes, as well as in chemical research. The compound's structure and properties make it a versatile building block for the development of various chemical compounds.

83482-80-8

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83482-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83482-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,8 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83482-80:
(7*8)+(6*3)+(5*4)+(4*8)+(3*2)+(2*8)+(1*0)=148
148 % 10 = 8
So 83482-80-8 is a valid CAS Registry Number.

83482-80-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N1-phenyl-N4-phenylsulfonyl-1,4-phenylenediamine

1.2 Other means of identification

Product number -
Other names Benzolsulfonsaeure-(4-anilino-anilid)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83482-80-8 SDS

83482-80-8Relevant academic research and scientific papers

REACTION OF UNSYMMETRICAL N1,N4-DISUBSTITUTED 1,4-BENZOQUINONE DIIMINES WITH HYDROGEN CHLORIDE

Burmistrov, K. S.,Yurchenko, A. G.

, p. 1722 - 1724 (2007/10/02)

The point of entry of chlorine into the molecules of unsymmetrical p-benzoquinone imines in their reaction with hydrogen chloride is determined by the comparative stability of the isomeric quinonoid intermediates, which can be assessed by means of an addi

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